Anderson, M. (1971). Family structure in nineteenth century Lancashire. Cambridge: Cambridge University Press.
Asche, G., Coyte, P.C., & Chan, B. (1996). The economic costs of musculoskeletal disorders for Canadian seniors (abstract). American Public Health Association 124th Annual Meeting and Exposition.
Badley, E.M., Rasooly, I., & Webster, G.K. (1994). Relative importance of musculoskeletal disorders as a cause of chronic health problems, disability and health care utilization: Findings from the 1990 Ontario Health Survey. Journal of Rheumatology, 21, 505–514.
Badley, E.M., Rothman, L.M., & Wang, P.P. (1998). Modeling physical dependence in arthritis: The relative contribution of specific disabilities and environmental factors. Arthritis Care and Research, 11, 335–346.
Baltes, M.M. (1995). The many faces of dependency in old age. Cambridge: Cambridge University Press.
Barnes, C., & Oliver, M. (1995) Disability politics: Understanding our past, changing our future. London: Routledge.
Blumer, H. (1969). Symbolic interactionism: Perspective and method. Englewood Cliffs, NJ: Prentice-Hall.
Bond, J. (1976). Dependency and the elderly: problems of conceptualization and measurement. In Munnichs, I., & van den heuvel, W. (Eds.), Dependency or interdependency in old age. (pp. 11–23). Hague: Martinus Nijhoff.
Braden, C.J. (1991) Learned response to chronic illness: disability payment recipients vs nonrecipients. Rehabilitation Psychology, 36(4), 265–277.
Brody, E.M. (1981). Women in the middle and family help to older people. The Gerontologist, 21, 470–480.
Brody, E.M., Johnsen, P.T., & Fulcomer, M.C. (1984). What should adult children do for elderly parents? Opinions and preferences of three generations of women. Journal of Gerontology, 39, 736–746.
Bury, M.R. (1988). Chronic illness as biographical disruption. Sociology of Health and Illness, 4, 167–182.
Bury, M.R. (1991). The sociology of chronic illness: A review of research and prospects. Sociology of Health and Illness, 13, 452–468.
Cantor, M.H. (1979). Neighbors and friends: An overlooked resource in the informal support system. Research on Aging, 1, 434–463.
Carricaburu, D., & Pierret, J. (1995) From biographical disruption to biographical reinforcement: the case of HIV-positive men. Sociology of Health and Illness, 17(1), 65–88.
Charmaz, K. (1983). Loss of self: a fundamental form of suffering in the chronically ill. Sociology of Health and Illness, 5(2), 168–195.
Charmaz, K. (1995). The body, identity and self: adapting to impairment. The Sociological Quarterly, 36(4), 657–680.
Corbin, J.M., & Strauss, A. (1988). Unending work and care: Managing chronic illness at home. San Francisco: Jossey-Bass Publishers.
Fife, B.L. (1994). The conceptualization of meaning in illness. Social Science and Medicine, 38(2), 309–316.
French, S. (1993). What's so great about independence? In Swain, J., Finkelstein, V., French, S., & Oliver, M. (Eds.), Disabling barriers-enabling environments (pp. 44–48). London: Sage Publications
Fries, J.J., Spitz, P., Kraines, R.G., & Holman, H.R. (1980). Measurement of patient outcomes in arthritis. Arthritis and Rheumatology, 23, 137–145.
Gignac, M.A.M., & Cott, C. (1998). A conceptual model of independence and dependence for adults with chronic physical illness and disability. Social Science and Medicine, 47, 739–753.
Goffman, E. (1963). Stigma. Englewood Cliffs, NJ.: Prentice-Hall.
Hahn, H. (1994). The minority group model of disability: Implications for medical sociology. Research in the Sociology of Health Care, 11, 3–24.
Kaufman, S.R. (1986). The ageless self: Sources of meaning in later life. Madison: University of Wisconsin Press.
Kaufman, S.R. (1993). Reflections on “The Ageless Self”. Generations, Spring /Summer, 13–16.
Kaufman, S.R. (1994). The social construction of frailty: An anthropological perspective. Journal of Aging Studies, 8, 45–58.
Keating, N., Fast, J., Oakes, L., & Harlton, S. (1996). Defining eldercare: Concepts and boundaries. Final report to NHRDP.
Lazarus, R.S., & Folkman, S. (1984). Stress appraisal and coping. New York: Springer.
Marshall, V.W., McMullin, J.A., Ballantyne, P., Daciuk, J., & Wigdor, B.T. (1995) Contributions to independence over the adult life course. Toronto: Centre for Studies of Aging, University of Toronto.
Martin Matthews, A., & Shipsides, A. (1989). Contributors to the loss of independence and the promotion of independence among seniors: Literature review and consultation with key informants. Report for the Seniors Independence Research Program: Community Health Division, Health and Welfare Canada. Guelph: Gerontology Research Centre, University of Guelph.
Miles, M.B., & Huberman, A.M. (1995) Qualitative data analysis (2nd ed.). London: Sage.
Oleson, V. (1990). Problematic bodies: Past, present and future. Symbolic Interaction, 17, 231–237.
Patton, M.Q. (1990) Qualitative evaluation and research methods (2nd ed.). New-bury Park, CA: Sage.
Pfeiffer, D. (1994). The Americans with Disabilities Act: costly mandates or civil rights? Disability and Society, 9, 533–542.
Pinder, R. (1990). What to expect: information and the management of uncertainty in Parkinson's disease. Disability Handicap & Society, 5(1), 77–92.
Pippin, K. (1996). A phenomenological analysis of the concept of normalization for the elderly and its value for understanding the design, commercialization and use of assisiivé mobility devices. Master of Science in Behavioural Science Thesis, University of Toronto.
Robinson, C.A. (1993). Managing life with a chronic condition: the story of normalization. Qualitative Health Research, 3(1), 6–28.
Rush, K.L., & Ouellet, L.L. (1997). Mobility aids and the elderly client. Journal of Gerontological Nursing, January, 7–15.
Stewart, D.C., & Sullivan, R.J. (1982). Illness behavior and the sick role in chronic disease: The case of multiple sclerosis. Social Science and Medicine, 16, 1397–1404.
Stone, D.A. (1984). The disabled state. Philadelphia: Temple University Press.
Verbrugge, L.M. (1990). The iceberg of disability. In Stahl, S.M. (Ed.), Longevity: health and health care in later life (pp. 55–75). Newbury Park, CA.: Sage.
Verbrugge, L.M., & Jette, A.M. (1994) The disablement process. Social Science and Medicine, 38(1), 1–14.
Verbrugge, L.M., Rennert, C., & Madans, J.H. (1997). The great efficacy of personal and equipment assistance in reducing disability. American Journal of Public Health, 87(3), 384–392.
Wiener, C.L., & Dodd, M.J. (1993). Coping amid uncertainty; an illness trajectory perspective. Scholarly Inquiry for Nursing Practice: An International Journal, 7(1), 17–31.
Wigdor, B.T., & Plouffe, L. (1992). Seniors independence: Whose responsibility? Ottawa: National Advisory Council on Aging, Forum Collection.
Wilkin, D. (1987). Conceptual problems in dependency research. Social Science and Medicine, 24, 867–873.
Williams, G.H. (1991). Disablement and the ideological crisis in health care. Social Science and Medicine, 31, 517–524.
Yoshida, K.K. (1997). Uncertainty in the lives of people with Spinal Cord Injury and Rheumatoid Arthritis. Canadian Journal of Rehabilitation, 10(1), 5–14.